Assessment of correlation between asthenozoospermia and mitochondrial DNA mutations in Egyptian infertile men

BACKGROUND: Asthenozoospermia is a chief reason for male seminal pathologies with an impression of around 19% of infertile patients. Spermatozoa mitochondrial DNA variations seem to link with low sperm motility. The objective of the study was to assess the relation between mitochondrial mutations an...

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Dades bibliogràfiques
Publicat a:J Genet Eng Biotechnol
Autors principals: Abd Elrahman, Mohamed M., El makawy, Aida I., Hassanane, Mohamed S., Alam, Sally S., Hassan, Nagwa H. A., Amer, Medhat K.
Format: Artigo
Idioma:Inglês
Publicat: Springer Berlin Heidelberg 2021
Matèries:
Research
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7813956/
https://ncbi.nlm.nih.gov/pubmed/33459881
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s43141-020-00111-0
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